breast cancer pathology Flashcards

1
Q

how has breast cancer rates changed over time

A

It has decreased in the last 20 years

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2
Q

breast cancer risk factors

A

Familial: BRCA1/BRCA2, Li Fraumeni syndrome (p53 mutation), Cowden syndrome (PTEN mutation), Peutz-Jeghers syndrome (STK11/LKB1 mutation). Sporadic: increasing age, young age at menarche, late menopause, hormonal, post-menopausal women, ionizing radiation, family history. Having a child earlier in life is protective

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3
Q

Functions of BRCA1 and 2, and cancers associated with them

A

•Both are tumor suppressor genes which facilitate DNA damage repair (loss of function progresses to cancer). BRCA1: breast cancer, ovarian cancer. BRCA2: breast cancer (males too), ovarian cancer

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4
Q

most common metastases to breast and who gets metastatic breast cancer

A

hematoogic, melanoma, lung, ovarian, kidney, prostate, stomach. • Curiously, in persons <20 yrs old metastatic lesions are more common than primary malignant lesions, but this is a very small subset of patients

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5
Q

Carcinoma in-situ

A

A general concept in neoplastic pathology where neoplastic epithelial cells grow within the confines of the basement membrane. The tumor has not yet become invasive

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6
Q

ductal carcinoma in situ histology

A

Clonal proliferation of epithelial cells within the ducts leaving the myoepithelial layer and basement membrane intact. Five classic histologic patterns include comedo (central necrosis), solid, cribriform (punched-out holes), papillary (large projections into the lumen) and micropapillary (small projections into the lumen)

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7
Q

DCIS presentation

A

calcifications seen on mammography. Generally asymptomatic and nonpalpable

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8
Q

DCIS grade

A

Comedo pattern contains central necrosis and is always high grade, other types range from low to high grade. 6. Low grades often express hormonal receptors (estrogen and progesterone), high grades often overexpress Her2/neu.

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9
Q

DCIS progression and risk of recurrence

A

DCIS is associated with a significant risk of developing invasive carcinoma. Risk factors for recurrence of DCIS include (1) histologic grade, (2) extent of breast involvement (size of DCIS), (3) if the DCIS is completely excised (if the margins are negative for DCIS)

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10
Q

DCIS treatment

A

Surgical excision (+/- other therapies) is curative in the vast majority of cases of tumors consisting purely of DCIS

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11
Q

Pagets disease

A

Neoplastic DCIS cells grow from the ducts onto the adjacent skin without invading through the basement membrane of the ducts or skin. Clinically presents as a scaly rash on the nipple. Many have associated invasive carcinoma including 1/3 who present without an associated mass and >9/10 of those with a mass. Prognosis depends on the presence of underlying carcinoma

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12
Q

Pagets histology

A

Paget cells= large cells in epidermis with clear halo

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13
Q

Lobular carcinoma in situ (LCIS)

A
  1. “Classic” LCIS always an incidental finding, does not form masses or calcifications. 2. Often multicentric and bilateral. 3. Patients are at a significantly increased risk for development of invasive carcinoma in both breasts (compared with DCIS were the higher risk is predominantly in the ipsalateral breast)
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14
Q

LCIS histology

A

small, uniform cells with round nuclei filling the lobules and poorly adhering to adjacent cells. 5. Some recognize a “pleomorphic” variant of LCIS that behaves more aggressively and some advocate treating these similar to DCIS

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15
Q

LCIS genetic alterations

A

The cells adhere to each other poorly because they have lost the function of important cell-cell adhesion molecules, chiefly e-cadherin.

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16
Q

Types of atypical hyperplasia

A

Technically not yet a carcinoma, but has some histologic features of in situ carcinoma. Can resemble DCIS, termed atypical ductal hyperplasia (ADH). Can resemble LCIS, termed atypical lobular hyperplasia (ALH). Both have increased risk of invasive carcinoma

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17
Q

Invasive carcinoma presentation

A

Commonly present as a palpable mass or as a mammographic abnormality. Uncommon presentations include an enlarged erythematous breast (termed “inflammatory carcinoma”) or as metastatic disease (typically an axillary lymph node). Advanced lesions fix the mass to the underlying chest wall and cause dimpling of the overlying skin.

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18
Q

Where does invasive carcinoma usually occur

A

Carcinoma most commonly occurs in the upper outer quadrant; these tumors spread first to axillary lymph nodes. When tumors occur in the inner quadrant they preferentially spread to the internal mammary lymph nodes

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19
Q

What causes inflammatory carcinoma

A

Diffuse involvement of dermal lymphatics (carries a poor prognosis)

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20
Q

invasive ductal carcinoma histology

A

Well-differentiated tumors contain well formed ducts with relatively bland appearing cells infiltrating a dense fibrous stroma. Poorly-differentiated tumors have either poorly formed ducts or no duct formation in which case they are composed of irregular groupings of markedly atypical appearing cells. Sheets, nests, cords or individual cells. DCIS alos occurs in up to 80%.

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21
Q

gene/ hormone expression in well vs poorly differentiated invasive ductal carcinoma

A

Well differentiated: Express hormone receptors (E and P). Poorly differentiated: less hormone receptors, tend to overexpress epidermal growth factor receptor HER2/neu

22
Q

Invasive ductal carcinoma presentation

A

firm, fibrous, rock hard mass with sharp margins.

23
Q

Invasive ductal carcinoma subgroups

A

a. Luminal A: Largest group. ER positive, HER2 negative. b. Luminal B: ER positive, HER2 positive. c. Normal breast-like: ER positive, HER2 negative just like “luminal A,” but their gene expression more closely resembles normal breast tissue. d. Basal like: ER and HER2 negative. Gene expression profile does not resemble epithelial cells, but more closely resembles myoepithelial cells and stem cells. e. HER2 positive: ER negative, HER2 positive.

24
Q

Invasive lobular carcinoma

A

second most common. Lost function of e-cadherin. Similar appearance as LCIS. individual tumor cells, sometimes in single file rows, infiltrating the stroma.

25
Q

Invasive lobular carcinoma receptors/ genes

A
  1. Generally express hormone receptors and negative for HER2/neu overexpression
26
Q

metastasis of lobular and ductal invasive carcinomas

A
  1. ILC tends to metastasize more frequently to CSF, G.I. tract, ovaries/uterus and peritoneum and less frequently to the lungs and pleura than ductal carcinomas
27
Q

invasive lobular carcinoma histology

A

•Tumor cells are small, uniform, round with minimal pleomorphism, evenly disbursed chromatin and no nucleoli (nuclear grade 1, like LCIS cells). Cells grow in single file (linear, single file). Cells grow in targetoid pattern of noncohesive cells encircling ducts. Cells loosely dispersed throughout fibrous matrix

28
Q

Tubular carcinoma presentation and prognosis

A

5th decade. Good prognosis

29
Q

Tbular carcinoma histology

A

Very well differentiated tumor composed of well-formed tubules and relatively bland appearing cells. Irregular angulated contours of glands. Open lumina with apocrine-like snouts and basophilic secretions
Columnar cell lesions in almost all cases with flat epithelial atypia . Desmoplastic stroma. invades fat. no basement membrane. no mitotic figures, necrosis.Very well differentiated tumor composed of well-formed tubules and relatively bland appearing cells. Irregular angulated contours of glands. Open lumina with apocrine-like snouts and basophilic secretions
Columnar cell lesions in almost all cases with flat epithelial atypia . Desmoplastic stroma. invades fat. no basement membrane. no mitotic figures, necrosis.Very well differentiated tumor composed of well-formed tubules and relatively bland appearing cells. Irregular angulated contours of glands. Open lumina with apocrine-like snouts and basophilic secretions
Columnar cell lesions in almost all cases with flat epithelial atypia . Desmoplastic stroma. invades fat. no basement membrane. no mitotic figures, necrosis.

30
Q

Tubular carcinoma hormones/ receptors

A

Almost all express hormone receptors and usually do not demonstrate HER2/neu overexpression

31
Q

Cribriform carcinoma

A

Subtype of tubular carcinoma that forms cribriform spaces in additional to well-formed tubules

32
Q

Tubular carcinoma is associated with…

A

low grade DCIS (micropapillary or cribriform)

33
Q

mucinous carcinoma presentation, histology, receptors/ genes

A
  1. Often presents as a well-circumscribed mass (mimicking a benign lesion) in relatively older age groups 2. Has a striking histologic appearance with small islands of tumor cells floating in pale-blue lakes of mucin. 3. Tumors usually express hormone receptors 4. More frequent in patients with BRCA1 mutation
34
Q

Medullary carcinoma

A

Well circumscribed mass. Negative for horomone receptors and Her2/Neu. More frequent in patients with BRCA1 mutation

35
Q

Medullary carcinoma histology

A

(1) indistinct cell borders (aka syncytial growth) at least 75% of tumor with large pleomorphic tumor cells containing large nuclei, prominent nucleoli, numerous mitotic figures (2) Prominent lymphoplasmacytic infiltrate at periphery (T-cells and IgA plasma cells) (3) Pushing borders / well circumscribed. (4) sparse stroma, giant cells, necrosis.

36
Q

Metaplastic carcinoma

A

•Any carcinoma with nonglandular growth (ie not properties typically by epithelial or myoepithelial cells). squamous, spindle cell or heterologous (pseudosarcomatous) differentiation. arise in association with poorly differentiated ductal carcinoma more often than other types.

37
Q

Metaplastic carcinoma histology

A

Divided into squamous and pseudosarcomatous. Most typical histology is focal squamous metaplasia in an otherwise typical invasive ductal carcinoma
Divided into squamous and pseudosarcomatous. Most typical histology is focal squamous metaplasia in an otherwise typical invasive ductal carcinoma

38
Q

Spindle cell carcinoma

A

subgroup of metaplastic squamous cell carcinoma with mostly (or entirely) spindled morphology

39
Q

Sarcomas

A

May arise in most organ systems (angiosarcoma, rhabdomyosarcoma, liposarcoma, etc.). 3. Tumors derived from blood vessels, angiosarcoma and lymphangiosarcoma, are among the most common primary breast sarcomas. These can arise (1) spontaneously, (2) following radiation therapy and (3) in the setting of chronic edema (Stewart-Treves syndrome)

40
Q

Breast lymphoma

A

May occur as primary breast lesions or disseminated disease may secondarily involve the breast. Most commonly patients present with a palpable mass or masses. Of primary lesions, non-Hodgkin lymphomas (NHLs) are the most frequent, of these, Diffuse large B-cell lymphomas are the most common

41
Q

Mixed (Biphasic) of the breast

A
  1. This category includes fibroadenoma (benign) and phyllodes tumors, both are composed of stromal and epithelial components and both arise from the stroma immediately surrounding the breast lobules (intralobular stroma)
42
Q

Phyllodes tumor

A
  1. stromal growths covered by epithelium often forming a leaf-like appearance (“phyllo” Greek for “leaf”). Do not typically metastasize. Only the stromal part is prone to mets. Large blky mass.
43
Q

Fibroadenoma

A

cellular myxoid stroma encircling glandular/cystic spaces. Small firm mass with sharp edges.

44
Q

Phyllodes tumor vs fibroadenoma

A

Phyllodes tumors differ from fibroadenomas by: mitotic rate, overgrowth of hypercellular stromal component, infiltrative boarders

45
Q

breast cancer prognostic factors

A

Primary breast lesion characteristics (size, invasion, inflammatory carcinoma, invading skin or skeletal muscle), Regional lymph node involvement, Examination for metastatic disease

46
Q

Breast cancer staging

A

For breast carcinoma: T: Tumor size and local growth characteristics. N: Extent of lymph node involvement. M: Presence of distant metastasis

47
Q

Hormone receptor prognosis

A

Expression of estrogen and progesterone receptors portends a better prognosis. Also more likely to respond to hormonally based therapy. HER2/neu overexpression is associated with poor prognosis.

48
Q

Which carcinomas have better vs worse prognosis

A

1.Tubular, mucinous and medullary carcinoma all have better prognosis than invasive ductal carcinoma.

49
Q

compare male breast cancer to females

A

similar risk factors, BRCA2 mutations increase risk for males. Association with Klinefelters syndrome. Most often present to the clinician as a subareolar palpable mass . Same histologic types. More often involve the chest wall and skin than female cancers. Expression of estrogen receptors is more common. Men often present at higher stage but prognosis is similar to women

50
Q

breast carcinoma pathogenesis

A

Site of origin is the terminal duct lobular unit. epithelial cells progress from proliferative disease to atypical hyperplasia to carcinoma in-situ to invasive carcinoma by accumulating genetic changes.